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Merck
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重要文件

533238

Sigma-Aldrich

邻氯苯甲醛肟

98%

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About This Item

線性公式:
ClC6H4CH=NOH
CAS號碼:
分子量::
155.58
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

98%

mp

73-76 °C (lit.)

官能基

amine
chloro
oxime

SMILES 字串

O\N=C\c1ccccc1Cl

InChI

1S/C7H6ClNO/c8-7-4-2-1-3-6(7)5-9-10/h1-5,10H/b9-5+

InChI 密鑰

FZIVKDWRLLMSEJ-WEVVVXLNSA-N

一般說明

2-Chlorobenzaldehyde oxime is also known as o-chlorobenzaldehyde oxime. It can be synthesized by reacting 2-chlorobenzaldehyde and hydroxylamine hydrochloride.

應用

2-Chlorobenzaldehyde oxime may be used in the preparation of:
  • 2-chlorobenzaldehyde under different reaction conditions
  • methyl 3-(2-chlorophenyl)-5-[1-(4-methoxybenzyloxy)-ethyl]isoxazole-4-carboxylate
  • dimethyl 3-(2-chlorophenyl)isoxazole-4,5-dicarboxylate
  • [3-(2-chlorophenyl)isoxazol-5-yl]methanol

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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Microwave-assisted chemoselective cleavage of oximes to their corresponding carbonyl compounds using 1, 3-dichloro-5, 5-dimethyl-hydantoin (DCDMH) as a new Deoximating reagent.
Khazaei A and Manesh AA.
Synthesis, 2005(12), 1929-1931 (2005)
Facile and Chemoselective Microwave-Assisted Cleavage of Oximes to Their Corresponding Carbonyl Compounds Using N,N?-Dibromo-N,N?-1,3-propylene-bis[(4-methylphenyl)sulfonamide] as a Deoximating Reagent.
Khazaei A, et al.
Synthesis, 2004(17), 2784-2786 (2004)
Design, synthesis and antibacterial activity of novel N-formylhydroxylamine derivatives as PDF inhibitors.
Yin L, et al.
Indian J. Chem. B, 50(5), 695-695 (2011)
Solid-phase synthesis of 5-isoxazol-4-yl-[1,2,4] oxadiazoles.
Quan C and Kurth M.
The Journal of Organic Chemistry, 69(5), 1470-1474 (2004)
A mild and selective method for the conversion of oximes into ketones and aldehydes by the use of N-bromophthalimide.
Khazaei A, et al.
J. Chem. Res. (M), 2004(10), 695-696 (2004)

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